Ionic Liquid Analogs of AlCl3 with Urea Derivatives as Electrolytes for Aluminum Batteries

The ionic liquid analog, formed through the mixture of urea and AlCl₃, has previously shown to serve as a low‐cost electrolyte for an aluminum‐graphite battery, while maintaining good performance and achieving high Coulombic efficiency. Undesirable are the relatively high viscosity and low conductivity of this electrolyte, when compared to chloroaluminate ionic liquids with organic cations. In this work, the fundamental changes to the electrolyte resulting from using derivatives of urea (N‐methyl urea and N‐ethyl urea), again mixed with AlCl₃, are examined. These electrolytes are shown to have significantly lower viscosities (η = 45, 67, and 133 cP when using N‐ethyl urea, N‐methyl urea, and urea, respectively, at 25 °C). The associated batteries exhibit higher intrinsic discharge voltages (2.04 and 2.08 V for N‐methyl urea and N‐ethyl urea electrolytes, respectively, vs 1.95 V for urea system@100 mA g^?1 specific current for ≈5 mg cm^?2 loading), due to changes in concentrations of ionic species. Aluminum deposition is directly observed to primarily occur through reduction of Al₂Cl₇^? when AlCl₃ is present in excess, in contrast to previously suggested cationic Al‐containing species, via operando Raman spectroscopy performed during cyclic voltammetry.     

A Water Stable,Near‐Zero‐Strain O3‐Layered Titanium‐Based Anode for Long Cycle Sodium‐Ion Battery

Layered transition metal (TM) oxides of the stoichiometry Na_xMO₂ (M = TM) have shown great promise in sodium‐ion batteries (SIBs); however, they are extremely sensitive to moisture. To date, most reported titanium‐based layered anodes exhibit a P2‐type structure. In contrast, O3‐type compounds are rarely investigated and their synthesis is challenging due to their higher percentage of unstable Ti³⁺ than the P2 type. Here, a pure phase and highly crystalline O3‐type Na_0.73Li_0.36Ti_0.73O₂ with high performance is successfully proposed in SIBs. This material delivers a reversible capacity of 108 mAh g^?1 with a stable and safe potential of 0.75 V versus Na/Na⁺. In situ X‐ray diffraction reveals that this material does not undergo any phase transitions and exhibits a near‐zero volume change upon Na⁺ insertion/de‐insertion, which ensures exceptional long cycle life over 6000 cycles. Importantly, it is found that this O3‐Na_0.73Li_0.36Ti_0.73O₂ shows superior moisture stability, even when immersed into water, which are both elusive for conventional layered TM oxides in SIBs. It is believed that the small interlayer distance and high occupation of interlayer vacancy promise such unprecedented water stability.     

Ferroelectric Poling of Methylammonium Lead Iodide Thin Films

Seemingly contradictory reports on polar domains and their origin have surrounded the controversial discussion about the ferroelectricity of the methyl ammonium lead iodide (MAPbI₃) thin films that are commonly employed in perovskite solar cells. In this work, microscopic modulations of the polar domain patterns upon application of an electric poling field are correlated with macroscopic changes to the currents through the MAPbI₃ layer. Piezoresponse force microscopy is used to monitor the widening, narrowing, generation or extinction of polar domains, as well as shifts of the domain walls at room temperature under an in‐plane electric poling field that is applied between two laterally organized electrodes. This poling leads to a net polarization of individual grains and the thin film itself. Macroscopically, this net polarization results in a persistent shift of the diode characteristics that is measured across the channel between the electrodes. Both the modulation of the polar domains upon electric poling and the concurrent persistent shift of the electric currents through the device are the unambiguous hallmarks of ferroelectricity, which demonstrate that MAPbI₃ is a ferroelectric semiconductor.     

Inrush current estimation and hot-swapping for safe parallel battery pack

ABSTRACT

Batteries used in electric vehicles and microgrid applications use battery modules connected in series to satisfy the voltage required for each system, and battery modules are connected in parallel to increase capacity. In this parallel connected system, in order to disconnect and reconnect a specific battery module or to reconnect a new battery module, the battery module to be newly connected should have a small state of charge (SOC) difference from the existing battery modules. In particular, when a new battery is to be connected under a load current, there is a problem that excessive inrush current may occur in a specific battery module due to the load current distributed to each module and the current due to the SOC difference. Therefore, in this paper, we propose a method of estimating the inrush current through an equivalent electrical modelling analysis for the case where a battery module is newly added in a system in which the battery modules are connected in parallel. In addition, the power management algorithm for the battery pack system with inrush current estimation is presented. The proposed method is validated through simulations and experiments of a battery pack system in which 10 battery modules of 710V and 120Ah are connected in parallel.     

基于单片机的双轴太阳能跟踪系统的设计

为了解决太阳能工程项目中光伏效率不高的问题,设计了双轴太阳能跟踪装置,该系统采用视日轨迹跟踪方案。文中着重分析了双轴跟踪的原理及其系统组成,利用光伏元件和STC89C52单片机实现大范围太阳跟踪,液晶显示屏实时显示最佳接收方位角及温湿度。在光线充足的天气条件下,跟踪装置自动旋转并始终保持太阳光垂直照射在太阳能电池的表面。在阴雨天或夜间等光线不足的条件下系统停止跟踪太阳转动。整个系统不需要任何外部电源供电,实现对太阳的高精度跟踪,并且使系统具有较强的抗干扰和运算能力。     

Large‐area epitaxial silicon solar cells based on industrial screen‐printing processes

Thin‐film epitaxial silicon solar cells are an attractive future alternative for bulk silicon solar cells incorporating many of the process advantages of the latter, but on a potentially cheap substrate. Several challenges have to be tackled before this potential can be successfully exploited on a large scale. This paper describes the points of interest and how IMEC aims to solve them. It presents a new step forward towards our final objective: the development of an industrial cell process based on screen‐printing for > 15% efficient epitaxial silicon solar cells on a low‐cost substrate. Included in the discussion are the substrates onto which the epitaxial deposition is done and how work is progressing in several research institutes and universities on the topic of a high‐throughput epitaxial reactor. The industrial screen‐printing process sequence developed at IMEC for these epitaxial silicon solar cells is presented, with emphasis on plasma texturing and improvement of the quality of the epitaxial layer. Efficiencies between 12 and 13% are presented for large‐area (98 cm²) epitaxial layers on highly doped UMG‐Si, off‐spec and reclaim material. Finally, the need for an internal reflection scheme is explained. A realistically achievable internal reflection at the epi/substrate interface of 70% will result in a calculated increase of 3 mA/cm² in short‐circuit current. An interfacial stack of porous silicon layers (Bragg reflectors) is chosen as a promising candidate and the challenges facing its incorporation between the epitaxial layer and the substrate are presented. Experimental work on this topic is reported and concentrates on the extraction of the internal reflection at the epi/substrate interface from reflectance measurements. Initial results show an internal reflectance between 30 and 60% with a four‐layer porous silicon stack. Resistance measurements for majority carrier flow through these porous silicon stacks are also included and show that no resistance increase is measurable for stacks up to four layers. Copyright © 2005 John Wiley & Sons, Ltd.     

太阳能路灯系统的优化配置

以太阳能路灯系统为例,提出优化方法．主要从能耗的降低、性能的稳定以及系统成本的减少人手,计算太阳能光伏组件和蓄电池容量,确定太阳能路灯系统优化配置的方法．同时系统实行智能控制,在保护蓄电池使用寿命的前提下,保证最大正常工作时间,从而提高太阳能路灯的节能性和经济性．     

基于纳米颗粒的铜锌锡硫硒薄膜制备

采用热注入法制备了Cu2ZnSnS4(CZTS)纳米颗粒,并形成高分散、稳定的"墨水",采用滴注方法形成CZTS前驱体薄膜。利用X射线衍射(XRD)、拉曼光谱(Raman)、透射电子显微镜(TEM)和紫外-可见光谱(UV-VIS)对CZTS纳米颗粒的晶体结构、表面形貌和带隙进行了表征。Raman数据显示合成的纳米颗粒为纯的CZTS,不存在ZnS和Cu2SnS3等杂相。傅里叶红外光谱(FTIR)和UV-VIS表明合成的CZTS纳米颗粒表面被油胺(OLA)包覆,并且其带隙为1.52 eV。对CZTS前驱体薄膜在硫化氢气氛和固态硒气氛中退火处理,得到铜锌锡硫硒(CZTSSe)薄膜。结果表明,经硫化氢处理后薄膜表面平整但CZTS晶粒并没长大,而经过固态硒处理后得到了结晶质量较好的CZTSSe薄膜。     

适用于200 mm太阳能电池片的闭管扩散/氧化系统设计

介绍了适用于太阳能电池生产线闭管磷扩散设备,着重阐述了该设备的结构组成、工艺原理及控制。     

Hybrid Perovskite Quantum Dot/Non-Fullerene Molecule Solar Cells with Efficiency Over 15%

Organic-inorganic hybrid film using conjugated materials and quantum dots (QDs) are of great interest for solution-processed optoelectronic devices, including photovoltaics (PVs). However, it is still challenging to fabricate conductive hybrid films to maximize their PV performance. Herein, for the first time, superior PV performance of hybrid solar cells consisting of CsPbI₃ perovskite QDs and Y6 series non-fullerene molecules is demonstrated and further highlights their importance on hybrid device design. In specific, a hybrid active layer is developed using CsPbI₃ QDs and non-fullerene molecules, enabling a type-II energy alignment for efficient charge transfer and extraction. Additionally, the non-fullerene molecules can well passivate the QDs, reducing surface defects and energetic disorder. The champion CsPbI₃ QD/Y6-F hybrid device has a record-high efficiency of 15.05% for QD/organic hybrid PV devices, paving a new way to construct solution-processable hybrid film for efficient optoelectronic devices.